Evidence map›Paper›PMID 42039507›Full record

ArticlebioRxiv : the preprint server for biology2026

Regional and Systemic Metabolic Remodeling Promotes Longevity by Bioengineered Yeast-Derived Lipids.

Yajuan Li, Zhiliang Bai, Yuhan Li, Fangyuan Gao, Shuo Qin, Jian Ran, Jorge Villazon, Anna Wang, Hongje Jang, Zhi Li and 6 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors.

Yajuan LiShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.ORCID 0000-0001-8687-0346
Zhiliang BaiDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.ORCID 0000-0002-3977-3057
Yuhan LiShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Fangyuan GaoDepartment of Ophthalmology, Center for Translational Vision Research, Gavin Herbert Eye Institute, University of California Irvine, Irvine, CA, USA 92697.ORCID 0000-0002-1270-8781
Shuo QinShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Jian RanDepartment of Molecular Biology, School of Biological Sciences, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Jorge VillazonShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.ORCID 0009-0006-8296-5894
Anna WangShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Hongje JangShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Zhi LiShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Shriya SankaranShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Yuting LiuDepartment of Molecular Biology, School of Biological Sciences, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Dorota Skowronska-KrawczykDepartment of Ophthalmology, Center for Translational Vision Research, Gavin Herbert Eye Institute, University of California Irvine, Irvine, CA, USA 92697.ORCID 0000-0002-5758-4225
Nan HaoDepartment of Molecular Biology, School of Biological Sciences, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.
Rong FanDepartment of Biomedical Engineering, Yale University, New Haven, CT 06520, USA.ORCID 0000-0001-7805-8059
Lingyan ShiShu Chien-Gene Lay Department of Bioengineering, University of California San Diego, 9450 Gilman Dr., La Jolla, CA, USA 92093.ORCID 0000-0003-1373-3206

Funding

HIPC Data Coordinating CenterU01AI167892 · NIAID · LA JOLLA INSTITUTE FOR IMMUNOLOGY · PI Steven H. Kleinstein, Bjoern Peters · 2022 to 2026
$18.7M
Yale TMC for Cellular Senescence in Lymphoid OrgansU54AG076043 · NIA · YALE UNIVERSITY · PI FAN, RONG, HALENE, STEPHANIE · 2021 to 2025
$7.0M
Yale Murine-TMC on Immune Cell Senescence Derived InflammationU54AG079759 · NIA · YALE UNIVERSITY · PI DIXIT, VISHWA DEEP, MONTGOMERY, RUTH R · 2022 to 2025
$6.5M
Network-Driven Dynamics of Replicative AgingR01AG056440 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEFF M HASTY, Nan Hao · 2017 to 2026
$5.6M
Reprogramming cell-fate decisions through predictive modeling and synthetic biologyR01GM144595 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAO, NAN, HASTY, JEFF M · 2022 to 2025
$2.8M
High-resolution High-speed Photoacoustic and Ultrasound Imaging of SmallVessel Functions in Ischemic StrokeR01NS111039 · NINDS · DUKE UNIVERSITY · PI YAO, JUNJIE · 2019 to 2023
$2.7M
Systems biology analysis of RNA-binding protein aggregation during cellular agingR01AG068112 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI HAO, NAN · 2021 to 2025
$2.3M
Engineered genetic clocks for control of cellular agingR01AG086348 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEFF M HASTY, Nan Hao · 2024 to 2026
$2.0M
Sugar Probed SRS Volumetric imaging of Metabolic ActivitiesR01GM149976 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Lingyan Shi · 2023 to 2026
$1.6M
Dynamical signaling and gene regulation in stress and agingR01AG093633 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Nan Hao · 2025 to 2026
$1.1M
Lympnoids tissue senescence and multimodal imaging using REDCATR01AG086548 · NIA · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI VISHWA DEEP DIXIT, Rong Fan · 2026 to 2026
$701k
Novel Optical Imaging Approach to Study Neurovascular Coupling SystemR21NS125395 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SHI, LINGYAN · 2022 to 2022
$435k
NIAID NIH HHS U01 AI167892NIA NIH HHS R01 AG056440NIA NIH HHS R01 AG068112NIA NIH HHS R01 AG086348NIA NIH HHS R01 AG086548NIA NIH HHS R01 AG093633NIA NIH HHS U54 AG076043NIA NIH HHS U54 AG079759NIGMS NIH HHS R01 GM144595NIGMS NIH HHS R01 GM149976NINDS NIH HHS R01 NS111039NINDS NIH HHS R21 NS125395
6 · The paper itself

Abstract

Aging is marked by a progressive breakdown of intestinal integrity and metabolic homeostasis, which together drives systemic decline in physiology and reduces lifespan. Here, we found that dietary lipids extracted from a genetically engineered long-lived yeast strain robustly extend lifespan in Drosophila and further uncovered the mechanisms using deuterium oxide-probed stimulated Raman scattering microscopy to image metabolic dynamics and single nucleus RNA sequencing (scRNA-seq) to unveil the underlying pathways. These yeast lipids are enriched in shorter, more saturated fatty acids and phospholipids as revealed by Raman spectroscopy and lipidomics, contributing to increased membrane order and reduced lipid storage. Functionally, targeted dietary supplementation with these lipid components synergistically prolongs fly lifespan. We show that these lipids reverse age-related declines in gut lipid droplet abundance, enhance membrane lipid incorporation, and increase de novo lipid synthesis, thereby improving epithelial structural integrity and barrier function. snRNA-seq identifies transcriptional remodeling in metabolically active enterocytes, including upregulation of autophagy and protein turnover genes, alongside reduction of unsaturated fatty acid biosynthesis. In the brain, dietary lipids orchestrate a dual metabolic strategy-promoting energy conservation and enhanced signaling across most neuronal and glial populations, while selectively boosting mitochondrial function in memory-critical Kenyon cells. All these leads to the enhancement of gut-to-glia communication, particularly through EGFR and FGFR pathways. Finally, analysis of our data with the Fly Metabolic Analysis Pipeline (FLY-MAP) reveals that yeast lipids restructure gut metabolic modules to coordinate energy production, redox balance, and nutrient flexibility. Our study uncovers a cross-kingdom mechanism of metabolic longevity regulation, paving the way for leveraging yeast-derived nutritional components to support tissue homeostasis and promote healthy aging.

Identifiers

PMID42039507
PMCPMC13104885

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.